Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Akiko, Nagata"'
Autor:
Mina Ishimaru PhD, Akiko Nagata MSc, Taichi Sato MSc, Doctoral Program Student, Ayano Sakai MSc, Satoko Suzuki PhD, Kentaro Kubota MSc
Publikováno v:
Gerontology and Geriatric Medicine, Vol 8 (2022)
Community building is necessary to help create a dementia-inclusive society. In this study, a one-of-a kind dementia education program based on mutual learning using instructional design was developed alongside community members and stakeholders. The
Externí odkaz:
https://doaj.org/article/fe3c7b68a414459898016685b572d242
Autor:
Yuka Kurokawa, Yusuke Kaida, Takuma Hazama, Yosuke Nakayama, Takaomi Otome, Ryo Shibata, Sakuya Ito, Goh Kodama, Nao Nakamura, Takatoshi Kambe, Tomofumi Moriyama, Akiko Nagata, Aki Minami, Ryotaro Ando, Yoshifumi Wada, Miki Sugiyama, Michiaki Usui, Michio Chiba, Atsuo Moriyama, Atsuko Ohara, Hiroshi Miyazaki, Tatsuyuki Kakuma, Kei Fukami
Publikováno v:
Renal Replacement Therapy, Vol 6, Iss 1, Pp 1-10 (2020)
Abstract Background Etelcalcetide is the first intravenously administered calcimimetic agent used to manage secondary hyperparathyroidism (SHPT) in hemodialysis (HD) patients. We evaluated the safety and efficacy of replacing cinacalcet with etelcalc
Externí odkaz:
https://doaj.org/article/44fc4637fec249aab21820b2c2f391c2
Autor:
Hironobu Fujisawa, Yosuke Nakayama, Shoichiro Nakao, Ryo Yamamoto, Yuka Kurokawa, Nao Nakamura, Akiko Nagata, Takahiro Tsukimura, Tadayasu Togawa, Hitoshi Sakuraba, Kei Fukami
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-8 (2019)
Abstract Background Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene, followed by deficiency in α-galactosidase A (α-gal) activity. Nephrotic syndrome, as the renal phenotype of FD, is unusual. Here,
Externí odkaz:
https://doaj.org/article/53d75e63bc8449fc985fddea2f46b27d
Autor:
Akiko Nagata, Kazuto Iijima, Ryota Sakamoto, Yuka Mizumoto, Miho Iwaki, Masaki Takiwaki, Yoshikuni Kikutani, Seketsu Fukuzawa, Minami Odagi, Masayuki Tera, Kazuo Nagasawa
Publikováno v:
Molecules, Vol 27, Iss 8, p 2427 (2022)
Blood levels of the vitamin D3 (D3) metabolites 25-hydroxyvitamin D3 (25(OH)D3), 24R,25-dihydroxyvitamin D3, and 1α,25-dihydroxyvitamin D3 (1,25(OH)2D3) are recognized indicators for the diagnosis of bone metabolism-related diseases, D3 deficiency-r
Externí odkaz:
https://doaj.org/article/d2238d20565c4872998ea88502ec583d
Autor:
Yuka Mizumoto, Ryota Sakamoto, Akiko Nagata, Suzuka Sakane, Atsushi Kittaka, Minami Odagi, Masayuki Tera, Kazuo Nagasawa
Publikováno v:
Biomolecules, Vol 12, Iss 1, p 69 (2022)
The active form of vitamin D3 (D3), 1a,25-dihydroxyvitamn D3 (1,25D3), plays a central role in calcium and bone metabolism. Many structure–activity relationship (SAR) studies of D3 have been conducted, with the aim of separating the biological acti
Externí odkaz:
https://doaj.org/article/aaba203519014043a1a5377b11ad9e7d
Autor:
Akiko, Nagata, Ryo, Nakamura
Publikováno v:
安田女子大学大学院紀要 = The journal of the Graduate School, Yasuda Women's University. 27:45-54
This research provides an overview of research on fostering the next generation in the context of childcare and identifies the limitations that need to be addressed. Having overviewed the previous research on how the intergenerational interaction aff
Autor:
Tadayasu Togawa, Yosuke Nakayama, Yusuke Kaida, Yuka Kurokawa, Takahiro Tsukimura, Takuma Hazama, Makoto Nasu, Hitoshi Sakuraba, Ryo Shibata, Kei Fukami, Akiko Nagata, Nao Nakamura, Seiji Saito
Publikováno v:
Nephrology Dialysis Transplantation
Fabry disease (FD), an X-linked lysosomal storage disorder caused by a deficiency in alfa-galactosidase A (α-Gal A) activity due to mutations in the GLA gene, has a prevalence of 0-1.69% in patients undergoing haemodialysis; however, its prevalence
Autor:
Haruki Ohshita, Toshiyuki Sakaki, Kaori Yasuda, Akiko Nagata, Yuka Mizumoto, Ryota Sakamoto, Miho Iwaki, Kazuo Nagasawa
Publikováno v:
ChemBioChem. 22:2896-2900
1α,25-Dihydroxyvitamin D3 (abbreviated here as 1,25D3 ) is a hormonally active form of vitamin D3 (D3 ), and is produced from D3 by CYP27 A1-mediated hydroxylation at C25, followed by CYP27B1-mediated hydroxylation at C1. Further hydroxylation of 25
Autor:
Nao Nakamura, Ryo Shibata, Yosuke Nakayama, Kei Fukami, Seiji Saito, Makoto Nasu, Hitoshi Sakuraba, Yuka Kurokawa, Tadayasu Togawa, Takahiro Tsukimura, Akiko Nagata, Yusuke Kaida, Takuma Hazama
Publikováno v:
Nephrology Dialysis Transplantation
Background Fabry disease (FD), an X-linked lysosomal storage disorder caused by a deficiency in alfa-galactosidase A (α-Gal A) activity due to mutations in the GLA gene, has a prevalence of 0–1.69% in patients undergoing haemodialysis; however, it
Autor:
Akiko, Nagata
Publikováno v:
安田女子大学大学院紀要 = The journal of the Graduate School, Yasuda Women's University. 26:31-39
This research considers the development and changes of Generativity, coined by E. H. Erikson, among youth and young adulthoods who are engaged in education and childcare and highlights the need of further empirical research which focuses on Generativ